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Arnaud Chevrollier
Affiliation : Centre National de la Recherche Scientifique · Inserm · Mitochondrial and Cardiovascular Physiopathology · Université d'Angers
- 4Publications (affiliation in France)
- 119Total publications
- 4317Citations
- 40h-index
Research profile
Arnaud Chevrollier has 4 indexed publications (2020–2026). Their work appears mainly in “Scientific Reports”, “Genes” and “Brain Communications”. Their most cited article, “Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophy” (2020), has been cited 52 times. Their work is co-authored with at least 12 researchers, including institutions in Morocco.
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Create my free profile Add my publicationsResearch areas
- Mitochondrial Function and Pathology
- Hereditary Neurological Disorders
- Metabolism and Genetic Disorders
- Autophagy in Disease and Therapy
- Cancer, Hypoxia, and Metabolism
Publications (4)
- Pathophysiological insights into ACO2-related inherited disorders through combined functional and multi-omic analyses of ACO2 patient-derived fibroblasts
- Next-Generation Sequencing Identifies Novel PMPCA Variants in Patients with Late-Onset Dominant Optic Atrophy
- DominantACO2mutations are a frequent cause of isolated optic atrophy
- Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophy
Publication venues
- Scientific Reports × 1
- Genes × 1
- Brain Communications × 1
- Neurology Genetics × 1
Publications per year
- 20261
- 20221
- 20211
- 20201
Collaborations
Partner institutions : Mohamed I University · Centre Hospitalier Universitaire d'Angers · Centre Hospitalier Universitaire de Montpellier · Clinique Jules Verne · Université de Montpellier
Co-authors’ countries : Morocco
Co-authors
- Guy Lenaers
- Naïg Guéguen
- Valérie Desquiret‐Dumas
- Dominique Bonneau
- Patrizia Amati‐Bonneau
- Céline Bris
- David Goudenège
- Majida Charif
- Pascal Reynier
- Isabelle Meunier
- Vincent Procaccio
- Xavier Zanlonghi
Bibliographic data from OpenAlex (open database).
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